YEM Search

搜索结果

PIGL

靶点ID:TCMBANKGE013379

靶点别名:CHIME

靶点描述:phosphatidylinositol glycan anchor biosynthesis class L

染色体:17

染色体位置:17p11.2

靶点类型:protein-coding

HERB_ID:HBTAR005250

HGNC_Link:8966

OMIM_Link:605947

Ensembl_Link:ENSG00000108474

靶点对应的植物

ID	拉丁名	药名	药用植物名	功能与主治	来源	药用部位	使用民族

靶点对应的化合物

化合物ID	化合物名	别名	分子式	分子质量	Smiles

靶点对应的疾病

疾病ID	疾病名	MeSH名	HPO名	UMLS名	疾病类型

TCMBANKDI001033	-	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI001342	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI001627	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI006622	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	Abnormality of prenatal development or birth; Abnormality of the cardiovascular system	Congenital Abnormality	disease
TCMBANKDI006900	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI007167	-	Abnormality of head or neck; Abnormality of the skeletal system	Anatomical Abnormality	phenotype
TCMBANKDI009422	-	-	Finding	phenotype
TCMBANKDI009697	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI010589	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI011000	Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases	Abnormality of the integument	Disease or Syndrome	disease
TCMBANKDI011456	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms; Cardiovascular Diseases	-	Disease or Syndrome	disease
TCMBANKDI011730	Eye Diseases; Nervous System Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI011845	-	-	Laboratory Procedure	phenotype
TCMBANKDI011883	-	-	Mental Process	phenotype
TCMBANKDI012023	Musculoskeletal Diseases	Abnormality of limbs	Finding	phenotype
TCMBANKDI012128	-	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI012637	-	Abnormality of limbs; Abnormality of the skeletal system	Finding	phenotype
TCMBANKDI013730	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	Abnormality of the cardiovascular system	Congenital Abnormality	disease
TCMBANKDI014539	Cardiovascular Diseases	Abnormality of the integument; Abnormality of the cardiovascular system	Finding	disease
TCMBANKDI016840	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases	Abnormality of the eye	Congenital Abnormality	disease
TCMBANKDI017183	-	Abnormality of the integument; Abnormality of head or neck	Finding	phenotype
TCMBANKDI018929	Eye Diseases	Abnormality of the eye	Disease or Syndrome	disease
TCMBANKDI019974	Skin and Connective Tissue Diseases	Abnormality of the integument	Finding	phenotype
TCMBANKDI023751	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the musculature	Finding	phenotype
TCMBANKDI024559	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI024846	-	Abnormality of the breast	Finding	phenotype
TCMBANKDI025616	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases	Abnormality of the cardiovascular system	Disease or Syndrome	disease
TCMBANKDI027324	-	Abnormality of head or neck	Finding	phenotype
TCMBANKDI029546	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases	Abnormality of head or neck	Congenital Abnormality	disease
TCMBANKDI031438	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Abnormality of the nervous system	Finding	phenotype
TCMBANKDI031570	-	Abnormality of the nervous system	Mental or Behavioral Dysfunction	disease
TCMBANKDI032109	Pathological Conditions, Signs and Symptoms	-	Disease or Syndrome	disease